United States · FDA National Drug Code directory

Dimethyl Fumarate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 70512-852_457243f3-2d22-3222-e063-6394a90ae21e
Product NDC: 70512-852
Form: CAPSULE, DELAYED RELEASE
Composition / generic term: Dimethyl Fumarate
Labeler: SOLA Pharmaceuticals, LLC
Marketing category: ANDA
Marketing start / end (source format): 20230131
Source listing expiry: 20261231

Source-listed ingredients

DIMETHYL FUMARATE — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE · 70512-852-14

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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